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Vital Signs 1013EU

by Carefusion Finland 320 Oy GUDID

Withdrawn United States

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403288302 UDI-DIDate26 Sep 2016ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Vital Signs
Generic Name
Electronic oesophageal stethoscope, single-use
Model / Ref / Catalog
1013EU
Primary DI / UDI-DI
10885403288302
FDA Product Code
FLL
GMDN Term
Electronic oesophageal stethoscope, single-use
Device Class
Class II
Regulation Number
880.2910
Commercial Distribution
Not in Commercial Distribution

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No